[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100639314":3},{"organization":4,"armGroups":7,"interventions":19,"overallOfficials":12,"centralContacts":25,"locations":12,"responsibleParty":31,"collaborators":35,"id":38,"slug":39,"hasResults":40,"nctId":41,"briefTitle":42,"officialTitle":42,"acronym":12,"eligibilityCriteria":43,"healthyVolunteers":40,"sex":44,"minAge":45,"maxAge":12,"enrollmentInfo":46,"targetDuration":12,"studyType":49,"phases":50,"briefSummary":52,"conditions":53,"keywords":55,"overallStatus":61,"whyStopped":12,"lastUpdateSubmitDate":62,"lastUpdatePostDateStruct":63,"startDateStruct":66,"completionDateStruct":68,"leadSponsor":70,"locationsCount":12},{"fullName":5,"class":6},"Fenerbahce University","OTHER",[8,13],{"label":9,"type":10,"description":11,"interventionNames":12},"Control Group","NO_INTERVENTION","Patients in the control group will be dressed in a traditional hospital gown.",null,{"label":14,"type":15,"description":16,"interventionNames":17},"Experimental Group","EXPERIMENTAL","Patients in this group will use the redesigned 100% cotton patient gown developed for abdominal surgery patients.",[18],"Device: Enhanced patient gown",[20],{"type":21,"name":22,"description":23,"armGroupLabels":24,"otherNames":12},"DEVICE","Enhanced patient gown","As part of the study, patients wearing the enhanced surgical gown will continue to wear the designated gown for at least 24 hours after achieving postoperative clinical stability (i.e., hemodynamically stable, awake, and able to move). The assessment will be conducted on the first postoperative day, within 24-48 hours after surgery. Following the completion of the enrollment period, data collection instruments will be administered to the patients. The opinions of healthcare professionals involved in the care and treatment of the enrolled patients (surgeons and surgical nurses) regarding the patient gown will be collected using the Patient Gown Evaluation Questionnaire for Healthcare Professionals.",[14],[26],{"name":27,"role":28,"phone":29,"phoneExt":12,"email":30},"Melis M CETINKAYA","CONTACT","+905354159839","melis.cetinkaya@fbu.edu.tr",{"type":32,"investigatorFullName":33,"investigatorTitle":34,"investigatorAffiliation":5,"oldNameTitle":12,"oldOrganization":12},"PRINCIPAL_INVESTIGATOR","Melis Merve Çetinkaya","LECTURER",[36],{"name":37,"class":6},"Bahçeşehir University","100639314","development-and-evaluation-of-the-effectiveness-of-patient-gowns-for-patients-undergoing-abdominal-surgery-100639314",false,"NCT07607457","Development and Evaluation of the Effectiveness of Patient Gowns for Patients Undergoing Abdominal Surgery","Patient Inclusion Criteria for the Study:\n\n* Be 18 years of age or older\n* Have undergone major abdominal surgery performed on an elective basis in a general surgery clinic (e.g., colorectal surgery, gastric surgery, hepatobiliary surgery, etc.)\n* Currently receiving care and treatment with medical devices (e.g., drains, Foley catheters, etc.)\n* Willing to participate in the study\n\nPatient Inclusion Criteria for the Study:\n\n* The participant refuses to wear a hospital gown\n* The participant has an allergy to the specified fabric Patients who are unable to mobilize for any reason (paralysis, general health impairment, history of stroke, etc.)\n* Patients with difficulty speaking and understanding Turkish\n* Patients lacking cognitive competence\n* Patients who develop complications within the first 24 hours after surgery and require revision surgery\n* Patients with prolonged intensive care unit (ICU) stays during the postoperative period\n* Since both the standard-sized traditional patient gown and the newly developed patient gown (available in sizes M-L) will be used in the study, patients whose body measurements do not fit within this size range will not be included in the study. This approach was adopted to prevent differences in comfort, mobility, and safety resulting from size mismatch from influencing the results, to ensure standardization in measurements, and to maintain comparability between the intervention and control groups.\n\nInclusion Criteria for Healthcare Professionals in the Study:\n\n* Providing care to patients who have undergone abdominal surgery\n* Having worked in the field for more than one year\n* Volunteering to participate in the study\n\nExclusion Criteria for Healthcare Professionals in the Study:\n\n• Being on leave or on sick leave during the study period.","ALL","18 Years",{"count":47,"type":48},172,"ESTIMATED","INTERVENTIONAL",[51],"NA","Traditional hospital gowns fail to protect patient privacy due to their design features, restrict freedom of movement and are incompatible with medical equipment. This situation negatively affects both patient satisfaction and the quality of care. The limited number of studies addressing this issue in the literature highlights the unique value of the topic. This project will be conducted with a randomized controlled design to develop a functional and ergonomic hospital gown suitable for clinical requirements for patients undergoing abdominal surgery and to evaluate its effectiveness. During the design process, priority will be given to privacy, ease of mobilization and integration with medical devices.\n\nThe study first plans to produce a prototype of a cotton fabric apron. Technical modeling will be conducted in collaboration with the Department of Textile and Fashion Design at Bahçeşehir University; the prototype will then be evaluated for clinical suitability. In the second phase, an experimental study will be conducted at Medicana Hospital in Ataşehir, Istanbul, to assess the apron's effectiveness. The sample size was determined using power analysis to include 86 patients in each of the control and intervention groups, for a total of 172 patients, and 14 healthcare professionals will participate in the study. Patient and healthcare professional identification forms, along with patient apron evaluation questionnaires, will be used as data collection tools.\n\nThe study consists of five main work packages: (1) obtaining the necessary permits and registering the research, (2) selecting materials and determining fabric properties, (3) technical modeling and design work, (4) patient trials, and (5) data analysis. Interdisciplinary collaboration will be maintained throughout the process, and the final model will be developed through iterative prototyping and pilot trials.\n\nThe widespread impact of the project is expected to increase the quality of clinical care by enhancing the comfort and safety of surgical patients, facilitating the workflow of healthcare professionals and promoting sustainable textile usage. In addition, the commercialization of the developed product has the potential to make an economic contribution to the domestic textile sector.",[54],"Abdominal Surgery Patients",[56,57,58,59,60],"Abdominal surgery","Patient gown","Functional design","Clinical care","Privacy","NOT_YET_RECRUITING","2026-05-22",{"date":64,"type":65},"2026-05-27","ACTUAL",{"date":67,"type":48},"2026-06-01",{"date":69,"type":48},"2026-12-31",{"name":5,"class":6}]